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Native collagen hydrogel nanofibres with anisotropic structure using core-shell electrospinning
Collagen hydrogel is a popular extracellular matrix (ECM) material in regenerative medicine and has an isotropic structure. In contrast, native ECM has an anisotropic structure. Electrospinning of collagen dissolved in organic solvents is widely used for fabricating anisotropic collagen nanofibres;...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5908855/ https://www.ncbi.nlm.nih.gov/pubmed/29674743 http://dx.doi.org/10.1038/s41598-018-24700-9 |
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author | Wakuda, Yuka Nishimoto, Shohei Suye, Shin-ichiro Fujita, Satoshi |
author_facet | Wakuda, Yuka Nishimoto, Shohei Suye, Shin-ichiro Fujita, Satoshi |
author_sort | Wakuda, Yuka |
collection | PubMed |
description | Collagen hydrogel is a popular extracellular matrix (ECM) material in regenerative medicine and has an isotropic structure. In contrast, native ECM has an anisotropic structure. Electrospinning of collagen dissolved in organic solvents is widely used for fabricating anisotropic collagen nanofibres; however, such fibres are water-soluble and require cross-linking before use as scaffolds for cell culture. Herein, electrospinning using a core-shell nozzle was employed to spin an aqueous acidic solution of collagen and encapsulate it within a shell of polyvinylpyrrolidone (PVP). Subsequently, the core collagen was gelled, and the shell PVP was washed away using a basic ethanol solution to yield anisotropic collagen hydrogel nanofibres. Immunostaining and Fourier transform infrared spectroscopy revealed that the obtained fibres were composed of collagen, and surface PVP was removed completely. Circular dichroism measurements confirmed that the fibres exhibited the triple helical structure characteristic of collagen. Human umbilical vein endothelial cells cultured on the collagen hydrogel fibres were oriented along the fibre direction. Hence, this method is suitable for fabricating fibrous anisotropic collagen hydrogels without chemical and thermal cross-linking, and can facilitate the development of safe medical materials with anisotropy similar to that of native ECM. |
format | Online Article Text |
id | pubmed-5908855 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-59088552018-04-30 Native collagen hydrogel nanofibres with anisotropic structure using core-shell electrospinning Wakuda, Yuka Nishimoto, Shohei Suye, Shin-ichiro Fujita, Satoshi Sci Rep Article Collagen hydrogel is a popular extracellular matrix (ECM) material in regenerative medicine and has an isotropic structure. In contrast, native ECM has an anisotropic structure. Electrospinning of collagen dissolved in organic solvents is widely used for fabricating anisotropic collagen nanofibres; however, such fibres are water-soluble and require cross-linking before use as scaffolds for cell culture. Herein, electrospinning using a core-shell nozzle was employed to spin an aqueous acidic solution of collagen and encapsulate it within a shell of polyvinylpyrrolidone (PVP). Subsequently, the core collagen was gelled, and the shell PVP was washed away using a basic ethanol solution to yield anisotropic collagen hydrogel nanofibres. Immunostaining and Fourier transform infrared spectroscopy revealed that the obtained fibres were composed of collagen, and surface PVP was removed completely. Circular dichroism measurements confirmed that the fibres exhibited the triple helical structure characteristic of collagen. Human umbilical vein endothelial cells cultured on the collagen hydrogel fibres were oriented along the fibre direction. Hence, this method is suitable for fabricating fibrous anisotropic collagen hydrogels without chemical and thermal cross-linking, and can facilitate the development of safe medical materials with anisotropy similar to that of native ECM. Nature Publishing Group UK 2018-04-19 /pmc/articles/PMC5908855/ /pubmed/29674743 http://dx.doi.org/10.1038/s41598-018-24700-9 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Wakuda, Yuka Nishimoto, Shohei Suye, Shin-ichiro Fujita, Satoshi Native collagen hydrogel nanofibres with anisotropic structure using core-shell electrospinning |
title | Native collagen hydrogel nanofibres with anisotropic structure using core-shell electrospinning |
title_full | Native collagen hydrogel nanofibres with anisotropic structure using core-shell electrospinning |
title_fullStr | Native collagen hydrogel nanofibres with anisotropic structure using core-shell electrospinning |
title_full_unstemmed | Native collagen hydrogel nanofibres with anisotropic structure using core-shell electrospinning |
title_short | Native collagen hydrogel nanofibres with anisotropic structure using core-shell electrospinning |
title_sort | native collagen hydrogel nanofibres with anisotropic structure using core-shell electrospinning |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5908855/ https://www.ncbi.nlm.nih.gov/pubmed/29674743 http://dx.doi.org/10.1038/s41598-018-24700-9 |
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